Canonical Allele Identifier: CA324957
Gene: SURF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 215233
ClinVar RCV Id: RCV000200389 RCV001168010 RCV002485308
dbSNP Id: rs373551988 rs2130015004
gnomAD v3: 9-133353855-G-A
gnomAD v4: 9-133353855-G-A
MyVariant Identifiers: chr9:g.133353855G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353855G>A , CM000671.2:g.133353855G>A GRCh38
NC_000009.10:g.135210531G>A NCBI36
NG_008477.1:g.7652C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.409C>T MANE Select ENSP00000361042.3:p.Arg137Trp
ENST00000371974.7:c.409C>T ENSP00000361042.3:p.Arg137Trp
ENST00000437995.1:n.355C>T
ENST00000495952.5:n.399C>T
ENST00000615505.4:c.82C>T ENSP00000482067.1:p.Arg28Trp
NM_001280787.1:c.82C>T NP_001267716.1:p.Arg28Trp
NM_003172.3:c.409C>T NP_003163.1:p.Arg137Trp
XM_011518942.1:c.82C>T XP_011517244.1:p.Arg28Trp
NM_003172.4:c.409C>T MANE Select NP_003163.1:p.Arg137Trp
Search 100 bp 5'
Search 100 bp 3'